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17687-74-0

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17687-74-0 Usage

Description

TRICYCLOHEXYLMETHANOL is a compound with a unique structure, characterized by its heat capacity when in a liquid-quenched glass state. This property has been measured using adiabatic calorimetry, which provides valuable insights into its thermal behavior and potential applications.

Uses

Used in Pharmaceutical Industry:
TRICYCLOHEXYLMETHANOL is used as a compound with potential pharmaceutical applications due to its unique heat capacity properties. These properties may be harnessed for the development of new drugs or drug delivery systems that require specific thermal characteristics.
Used in Material Science:
In the field of material science, TRICYCLOHEXYLMETHANOL is used as a component in the development of advanced materials with specific thermal properties. Its heat capacity characteristics can be exploited to create materials with tailored thermal responses, which can be useful in various applications such as thermal management, insulation, or energy storage.
Used in Chemical Research:
TRICYCLOHEXYLMETHANOL serves as a subject of interest in chemical research, where its unique heat capacity properties can be further explored and understood. This knowledge can lead to the discovery of new chemical reactions, processes, or applications that capitalize on the compound's thermal behavior.
Used in Energy Industry:
In the energy industry, TRICYCLOHEXYLMETHANOL can be used as a component in the development of materials or systems that require specific heat capacity characteristics. This can be particularly useful in applications involving energy storage, heat management, or thermal insulation.
Used in Manufacturing Processes:
TRICYCLOHEXYLMETHANOL may be utilized in manufacturing processes that require materials with specific heat capacity properties. Its unique characteristics can be integrated into the production of various products, potentially improving their performance or efficiency in specific applications.

Synthesis Reference(s)

Journal of the American Chemical Society, 89, p. 2737, 1967 DOI: 10.1021/ja00987a042

Check Digit Verification of cas no

The CAS Registry Mumber 17687-74-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,8 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17687-74:
(7*1)+(6*7)+(5*6)+(4*8)+(3*7)+(2*7)+(1*4)=150
150 % 10 = 0
So 17687-74-0 is a valid CAS Registry Number.
InChI:InChI=1/C19H34O/c20-19(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h16-18,20H,1-15H2

17687-74-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name TRICYCLOHEXYLMETHANOL

1.2 Other means of identification

Product number -
Other names Hydroxy-tricyclohexyl-methan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:17687-74-0 SDS

17687-74-0Relevant articles and documents

The First Phase-transfer catalysed Reactions of Trialkylboranes. A Highly Facile Synthesis of Trialkylmethanols from Alkenes

Junchai, Bai,Hongxun, Ding

, p. 323 (2007/10/02)

The phase-transfer catalysed reactions of trialkylboranes, generated in situ via hydroboration of alkenes, with chloroform and aqueous sodium hydroxide, followed by treatment with hydrogen peroxide, provide an economic and convenient metod for the synthesis of trialkylmethanols.

Synthesis of Ketones and Tertiary Alcohols from Trialkylboranes. Use of Lithium Tris(phenylthio)methanide

Pelter, Andrew,Rao, J. Madhusudhana

, p. 1149 - 1150 (2007/10/02)

The interaction of lithium tris(phenylthio)methanide with trialkylboranes followed by oxidation allows the production of ketones or tertiary alcohols in good yields under mild conditions.

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